ClinVar Miner

List of variants in gene MYO1C reported as likely benign for not provided

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_001080779.2(MYO1C):c.1798-11T>C rs75255685 0.02316
NM_001080779.2(MYO1C):c.906+83C>T rs142965600 0.01899
NM_001080779.2(MYO1C):c.-117C>G rs74829228 0.01772
NM_001080779.2(MYO1C):c.2802G>A (p.Lys934=) rs45598333 0.01720
NM_001080779.2(MYO1C):c.2366+20G>A rs115264891 0.01272
NM_001080779.2(MYO1C):c.1021-23G>A rs115442427 0.01268
NM_001080779.2(MYO1C):c.906+84G>A rs148984607 0.01117
NM_001080779.2(MYO1C):c.76-31C>T rs72818298 0.01101
NM_001080779.2(MYO1C):c.906+71_906+72insTA rs1555521812 0.01084
NM_001080779.2(MYO1C):c.2611-18C>A rs45541839 0.01064
NM_001080779.2(MYO1C):c.231+55C>T rs11868607 0.00817
NM_001080779.2(MYO1C):c.231+39C>T rs45508597 0.00750
NM_001080779.2(MYO1C):c.1093-86G>A rs138121605 0.00725
NM_001080779.2(MYO1C):c.2760+11G>A rs45508699 0.00682
NM_001080779.2(MYO1C):c.2574A>C (p.Lys858Asn) rs61753652 0.00630
NM_001080779.2(MYO1C):c.2366+36A>G rs564948039 0.00601
NM_001080779.2(MYO1C):c.2760+37G>A rs113467106 0.00404
NM_001080779.2(MYO1C):c.2353C>A (p.Gln785Lys) rs140604493 0.00383
NM_001080779.2(MYO1C):c.1797+53A>G rs112303325 0.00366
NM_001080779.2(MYO1C):c.2213-62G>A rs151034773 0.00364
NM_001080779.2(MYO1C):c.2004C>T (p.Tyr668=) rs78672478 0.00338
NM_001080779.2(MYO1C):c.336G>C (p.Val112=) rs61756682 0.00335
NM_001080779.2(MYO1C):c.859G>A (p.Val287Ile) rs117696188 0.00290
NM_001080779.2(MYO1C):c.3065+31C>T rs45484695 0.00244
NM_001080779.2(MYO1C):c.319G>A (p.Val107Ile) rs140549082 0.00210
NM_001080779.2(MYO1C):c.1779C>G (p.Asp593Glu) rs201137128 0.00154
NM_001080779.2(MYO1C):c.2251C>T (p.Arg751Trp) rs150948604 0.00150
NM_001080779.2(MYO1C):c.177C>T (p.Ser59=) rs146239773 0.00145
NM_001080779.2(MYO1C):c.189C>T (p.Phe63=) rs45628238 0.00144
NM_001080779.2(MYO1C):c.518G>A (p.Arg173Gln) rs148694544 0.00094
NM_001080779.2(MYO1C):c.1241C>T (p.Thr414Ile) rs143802377 0.00091
NM_001080779.2(MYO1C):c.2385C>T (p.Val795=) rs199710927 0.00089
NM_001080779.2(MYO1C):c.249C>G (p.Val83=) rs147453285 0.00088
NM_001080779.2(MYO1C):c.1764G>C (p.Arg588=) rs149926987 0.00042
NM_001080779.2(MYO1C):c.1548T>C (p.Thr516=) rs138469522 0.00039
NM_001080779.2(MYO1C):c.561C>T (p.Ala187=) rs74777662 0.00030
NM_001080779.2(MYO1C):c.808-4C>T rs748712532 0.00016
NM_001080779.2(MYO1C):c.2817G>A (p.Gln939=) rs137985633 0.00013
NM_001080779.2(MYO1C):c.3150C>T (p.Asn1050=) rs139599214 0.00011
NM_001080779.2(MYO1C):c.3072G>A (p.Thr1024=) rs775198165 0.00009
NM_001080779.2(MYO1C):c.594C>T (p.Phe198=) rs201401570 0.00003
NM_001080779.2(MYO1C):c.1044G>A (p.Thr348=) rs994003614 0.00002
NM_001080779.2(MYO1C):c.1575-8A>G rs371291004 0.00002
NM_001080779.2(MYO1C):c.222T>C (p.Asn74=) rs760544139 0.00002
NM_001080779.2(MYO1C):c.628-3C>T rs754963919 0.00002
NM_001080779.2(MYO1C):c.843G>T (p.Lys281Asn) rs774390905 0.00001
NM_001080779.2(MYO1C):c.1020+42C>G rs113932235
NM_001080779.2(MYO1C):c.1092+23G>A rs78481682
NM_001080779.2(MYO1C):c.1212+19C>G rs76826401
NM_001080779.2(MYO1C):c.1296-12_1296-10del rs566181068
NM_001080779.2(MYO1C):c.1716+22C>G rs374746077
NM_001080779.2(MYO1C):c.1797+20G>C rs2286872
NM_001080779.2(MYO1C):c.231+48A>C rs376048640
NM_001080779.2(MYO1C):c.2415C>T (p.Asn805=)
NM_001080779.2(MYO1C):c.2853G>A (p.Glu951=) rs138350458
NM_001080779.2(MYO1C):c.3065+46_3065+47del rs368437001
NM_001080779.2(MYO1C):c.313C>T (p.Arg105Cys)
NM_001080779.2(MYO1C):c.318C>T (p.Gly106=)
NM_001080779.2(MYO1C):c.759C>G (p.Arg253=) rs45614232

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